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The complete sequence of this research compound is: Tyr-Leu-Arg-Ile-Val-Gln-Cys-Arg-Ser-Val-Glu-Gly-Ser-Cys-Gly-Phe, with a disulphide bond between the two cysteine residues (Cys-7 and Cys-15) that contributes significantly to the structural stability of the peptide loop conformation

(2014) documented that the compound remains stable in aqueous buffers at pH 4.57.4 for at least two weeks even at 60C stress conditions, though oxidative stress represents its greatest vulnerability

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Our oral peptides provide a convenient way to harness these potential benefits

It is also essential for DNA synthesis